Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs5918 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24